catalog number :
MBS7026293
products type :
Recombinant Protein
products full name :
Recombinant Mouse Myelin proteolipid protein (Plp1)
products short name :
[Myelin proteolipid protein (Plp1)]
other names :
[myelin proteolipid protein isoform 2; Myelin proteolipid protein; myelin proteolipid protein; proteolipid protein (myelin) 1; Lipophilin]
products gene name :
[Plp1]
products gene name syn :
[Plp]
other gene names :
[Plp1; Plp1; jp; Plp; msd; rsh; DM20; jimpy; Plp; PLP]
uniprot entry name :
MYPR_MOUSE
host :
Cell Free Expression
sequence positions :
[2-277. Full Length of Mature Protein]
sequence :
GLLECCARCLVGAPFASLVATGLCFFGVALFCGCGHEAL
TGTEKLIETYFSKNYQDYEYLINVIHAFQYVIYGTASFF
FLYGALLLAEGFYTTGAVRQIFGDYKTTICGKGLSATVT
GGQKGRGSRGQHQAHSLERVCHCLGKWLGHPDKFVGITY
ALTVVWLLVFACSAVPVYIYFNTWTTCQSIAFPSKTSAS
IGSLCADARMYGVLPWNAFPGKVCGSNLLSICKTAEFQM
TFHLFIAAFVGAAATLVSLLTFMIAATYNFAVLKLMGRG
TKF
form :
Liquid containing glycerol
storage stability :
Store at -20 degree C, for extended storage, conserve at -20 degree C or -80 degree C. Repeated freezing and thawing is not recommended. Store working aliquots at 4 degree C for up to one week.
app notes :
This is a recombinant transmembrane protein expressed in a cell-free expression system.
other info1 :
Species: Mouse. Storage Buffer: Tris-based buffer, 50% glycerol.
products categories :
Transmembrane Protein
ncbi acc num :
NP_001277490.1
ncbi gb acc num :
NM_001290561.1
ncbi mol weight :
26,274 Da
uniprot summary :
PLP1: This is the major myelin protein from the central nervous system. It plays an important role in the formation or maintenance of the multilamellar structure of myelin. Defects in PLP1 are the cause of leukodystrophy hypomyelinating type 1 (HLD1); also known as Pelizaeus-Merzbacher disease. HLD1 is an X-linked recessive dysmyelinating disorder of the central nervous system in which myelin is not formed properly. It is characterized clinically by nystagmus, spastic quadriplegia, ataxia, and developmental delay. Defects in PLP1 are the cause of spastic paraplegia X- linked type 2 (SPG2). SPG2 is characterized by spastic gait and hyperreflexia. In some patients, complicating features include nystagmus, dysarthria, sensory disturbance, mental retardation, optic atrophy. Belongs to the myelin proteolipid protein family. 2 isoforms of the human protein are produced by alternative splicing. Protein type: Membrane protein, multi-pass; Cell surface; Membrane protein, integral. Cellular Component: integral to membrane; membrane; myelin sheath; plasma membrane. Molecular Function: protein binding; structural constituent of myelin sheath; structural molecule activity. Biological Process: astrocyte development; axon ensheathment; cell maturation; glial cell differentiation; inflammatory response; integrin-mediated signaling pathway; long-chain fatty acid biosynthetic process; myelination; myelination in the central nervous system